Kết quả tìm kiếm - Martin Barron
- Đang hiển thị 1 - 16 kết quả của 16
-
1
-
2
Identifying and removing the cell-cycle effect from single-cell RNA-Sequencing data Bằng Martin Barron, Jun Li
Được phát hành 2016Artigo -
3
Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia Bằng Martin Barron, Sinéad McDonnell, I C Mackie, Michael J. Dixon
Được phát hành 2008Revisão -
4
-
5
-
6
-
7
-
8
Entry Mechanisms of Herpes Simplex Virus 1 into Murine Epidermis: Involvement of Nectin-1 and Herpesvirus Entry Mediator as Cellular Receptors Bằng Philipp Petermann, Katharina Thier, Elena Rahn, Frazer J. Rixon, Wilhelm Bloch, Semra Özçelik, Claude Krummenacher, Martin Barron, Michael J. Dixon, Stefanie Scheu, Klaus Pfeffer, Dagmar Knebel-Mörsdorf
Được phát hành 2014Artigo -
9
Mitochondrial DNA Defects and Selective Extraocular Muscle Involvement in CPEO Bằng Laura C. Greaves, Patrick Yu‐Wai‐Man, Emma L. Blakely, Kim J. Krishnan, Nina E. Beadle, Jamie Kerin, Martin Barron, Philip G. Griffiths, Alison Dickinson, Douglass M. Turnbull, Robert W. Taylor
Được phát hành 2010Artigo -
10
Mitochondrial DNA mutations in human colonic crypt stem cells Bằng Robert W. Taylor, Martin Barron, Gillian M. Borthwick, Amy Gospel, Patrick F. Chinnery, David C. Samuels, Geoffrey A. Taylor, Stefan M. Plusa, Stephanie Needham, Laura C. Greaves, Thomas B. L. Kirkwood, Douglass M. Turnbull
Được phát hành 2003Artigo -
11
A homoplasmic mitochondrial transfer Ribonucleic Acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy Bằng Robert W. Taylor, Carla Giordano, Mercy M. Davidson, Giulia d’Amati, H H Bain, Christine Hayes, Helen Leonard, Martin Barron, Carlo Casali, Filippo M. Santorelli, Michio Hirano, Robert N. Lightowlers, Salvatore DiMauro, Douglass M. Turnbull
Được phát hành 2003Artigo -
12
Mitochondrial DNA mutations are established in human colonic stem cells, and mutated clones expand by crypt fission Bằng Laura C. Greaves, Sean Preston, Paul Tadrous, Robert W. Taylor, Martin Barron, Dahmane Oukrif, Simon J. Leedham, Maesha Deheragoda, Peter Sasieni, Marco Novelli, Janusz Jankowski, Douglass M. Turnbull, Nicholas A. Wright, Stuart A.C. McDonald
Được phát hành 2006Artigo -
13
Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome Bằng James O’Sullivan, Carolina Cavalcante Bitu, Sarah B. Daly, Jill Urquhart, Martin Barron, Sanjeev S. Bhaskar, Hercílio Martelli‐Júnior, Pedro Eleutério dos Santos Neto, M. Adela Mansilla, Jeffrey C. Murray, Ricardo D. Coletta, Graeme Black, Michael J. Dixon
Được phát hành 2011Artigo -
14
Mast cell activation test in the diagnosis of allergic disease and anaphylaxis Bằng Rajia Bahri, Adnan Čustović, Peter Korošec, Marina Tsoumani, Martin Barron, Jiakai Wu, Rebekah Sayers, Alf Weimann, Mónica Ruiz-García, Nandinee Patel, Abigail Robb, Mohamed H. Shamji, Sara Fontanella, Mira Šilar, E. N. Clare Mills, Angela Simpson, Paul Turner, Silvia Bulfone‐Paus
Được phát hành 2018Artigo -
15
CNS-Native Myeloid Cells Drive Immune Suppression in the Brain Metastatic Niche through Cxcl10 Bằng Ian H. Guldner, Qingfei Wang, Lin Yang, Samantha M. Golomb, Zhuo Zhao, Jacqueline Lopez, Abigail Brunory, Erin N. Howe, Yizhe Zhang, Bhavana Palakurthi, Martin Barron, Hongyu Gao, Xiaoling Xuei, Yunlong Liu, Jun Li, Danny Z. Chen, Gary E. Landreth, Siyuan Zhang
Được phát hành 2020Artigo -
16
Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta Bằng David Parry, Steven J. Brookes, Clare V. Logan, James A. Poulter, Walid El‐Sayed, Suhaila Al‐Bahlani, Sharifa Al-Harasi, Jihad Sayed, El Mostafa Raïf, Richard F. Shore, Mayssoon Dashash, Martin Barron, Joanne Morgan, Ian Carr, Graham R. Taylor, Colin A. Johnson, Michael J. Aldred, Michael J. Dixon, J. Tim Wright, Jennifer Kirkham, Chris F. Inglehearn, Alan J. Mighell
Được phát hành 2012Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Genetics
Gene
Medicine
Mitochondrial DNA
Mitochondrion
Anatomy
Cell biology
Mutation
Enamel paint
Endocrinology
Molecular biology
Amelogenesis imperfecta
Cell
Cytochrome c oxidase
Dentistry
Heteroplasmy
Immunology
Internal medicine
Mitochondrial myopathy
Ameloblast
Biochemistry
Cell adhesion
Crypt
Dentinogenesis imperfecta
Heart failure
Human mitochondrial genetics
Immune system
Mast cell
Materials science